{{Rsnum
|rsid=397509383
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;CC)
|geno3=(CC;CC)
|Gene=FKBP10
|position=41820961
|Gene_s=FKBP10
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GA
|CHROM=17
|CLNACC=RCV000034324.3; RCV000034359.2
|CLNALLE=1
|CLNDBN=Bruck syndrome 1; Osteogenesis imperfecta type 11
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1850168:259450:2771; C3151218:613849:666
|CLNHGVS=NC_000017.10:g.39977213_39977214delCCinsA
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607063.0009
|Disease=Bruck syndrome 1; Osteogenesis imperfecta type 11
|FwdALT=A
|FwdREF=CC
|REF=GCC
|RSPOS=39977212
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397509383
|GENEINFO=FKBP10:60681
|GENE_ID=60681
|GENE_NAME=FKBP10
}}